A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv233e199



Internal ID22758006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92290479..92294811hg38UCSC Ensembl
chr11:92023645..92027977hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384333
hg194333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659996, esv2673286
SamplesHG00318, HG00251, HG00158, HG00106, NA20342, HG00250, HG00310
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv233e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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